Methyl iodide → (+/-)-Methyl N,N'-dibenzyloxycarbonylpiperazine-2-carboxylate

HRID 582227Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 582227
[CH2:1]([O:8][C:9]([N:11]1[CH2:16][CH2:15][N:14]([C:17]([O:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[O:18])[CH2:13][CH:12]1[C:27]([OH:29])=[O:28])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CI.[C:32](=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[CH2:1]([O:8][C:9]([N:11]1[CH2:16][CH2:15][N:14]([C:17]([O:19][CH2:20][C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)=[O:18])[CH2:13][CH:12]1[C:27]([O:29][CH3:32])=[O:28])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Komponenten

5

Edukt 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 226328591,4-Bis(benzyloxycarbonyl)piperazine-2-carboxylic acid

Produkt 1

HCID 21847669(+/-)-Methyl N,N'-dibenzyloxycarbonylpiperazine-2-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a flask containing N,N'-dibenzyloxycarbonylpiperazine-2-carboxylic acid (Step 1, 12.83 g, 32.20 mmol) dissolved in dry DMF (50 mL) is added methyl iodide (5.6 mL, 90.00 mmol) and potassium carbonate (4.60 g, 32.20 mmol). The mixture is stirred for 4 hours at ambient temperature under an inert atmosphere. The reaction is concentrated in vacuo, diluted with ethyl acetate (150 mL), washed with water (3×50 mL) and saline, dried over MgSO4, concentrated in vacuo, and chromatographed on silica gel (70-230 mesh), eluting with hexane/ethyl acetate (50/50). The appropriate fractions are combined (Rf =0.55, TLC, hexane/ethyl acetate, 50/50) and concentrated in vacuo to give the title compound, NMR (CDCl3) 7.31, 5.15, 5.12, 4.70, 4.1-2.9.

Aufarbeitung

  1. concentrationThe reaction is concentrated in vacuo
  2. additiondiluted with ethyl acetate (150 mL)
  3. washwashed with water (3×50 mL) and saline
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo
  6. customchromatographed on silica gel (70-230 mesh)
  7. washeluting with hexane/ethyl acetate (50/50)
  8. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-a626d09972e949b49600f0b7114a58f7
Quelldatensatz
uspto-grants-1999_07
Patentnummer
US05922707

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